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Since the beginning of time, people have been making a living by selling items to the public. Whether it is a lemonade stand, a stall at a market or an ecommerce store on Amazon. According to some studies, it is more profitable for businesses in America to offer free samples than discounts and money-saving coupons. In order for this theory to work, though, suppliers must be able to provide goods of high quality at low cost. This means that there is just one obstacle that prevents companies from offering free samples: manufacturing costs. Since the 1970s, online businesses have been offering free samples in order to increase conversion rates. This strategy has been incredibly successful. Recently, however, word about this method spread and many companies shied away from offering free samples. This is because of two things: people started thinking that free samples were a bad way to sell and more importantly, they realized that sending out free samples does not guarantee that you will pass the quality control tests set by the FDA and Food and Drug Administration (FDA).The FDA is a federal agency whose primary objective is to protect public health and safety by ensuring the safety of food and drugs while simultaneously maintaining standards of quality. The FDA does this by ensuring that all drugs are safe for human consumption. This means that the FDA closely monitors the entire drug development process. From the moment a drug company proposes a new drug to the time it is approved for public consumption, the FDA will be making sure that it meets their safety standards.During this approval process, any company looking to put out mass-produced drugs must prove to the FDA that their drug meets all quality safety standards; otherwise, they simply will not allow it on the market. It is important for companies to understand that once they are put on FDA’s radar, they will require every product to undergo thorough analysis before they can be allowed onto store shelves. For every newly launched product, the company will be required to submit a sample of their drug, and if it fails to pass the FDA’s inspection, they will not allow it on retail shelves.The first thing that the FDA does is test for quality and effectiveness. They first test for quality and make sure that all of the ingredients are uniformly mixed and correctly dosed; they also run tests for efficacy, which means to see whether the drug actually works as intended or has any adverse side-effects. Once this is done, they then proceed to examine each batch of drugs as it hits store shelves. There are three ways that the FDA checks to make sure products are both safe and effective. First, they test for chemical content; they do this by examining each batch of the ingredients against a database which has been created from formulas of earlier batches. If everything checks out, they move on. If there is a problem, however, they send it back to the manufacturer for further testing. After checking for chemical content, the FDA then tests for identity and strength.

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